Plasminogen activator inhibitor-1

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Serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
1OC0.png
PAI-1 in complex with the SMB domain of Vitronectin PDB 1OC0
Identifiers
Symbol(s) SERPINE1; PAI; PAI-1; PAI1; PLANH1
External IDs OMIM: 173360 MGI97608 Homologene68070
RNA expression pattern

PBB GE SERPINE1 202627 s at tn.png

PBB GE SERPINE1 202628 s at tn.png

More reference expression data

Orthologs
Human Mouse
Entrez 5054 18787
Ensembl ENSG00000106366 ENSMUSG00000037411
Uniprot P05121 Q7TPE9
Refseq NM_000602 (mRNA)
NP_000593 (protein)
NM_008871 (mRNA)
NP_032897 (protein)
Location Chr 7: 100.56 - 100.57 Mb Chr 5: 137.35 - 137.36 Mb
Pubmed search [1] [2]

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [3]

Please Take Over This Page and Apply to be Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [4] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Plasminogen activator inhibitor-1 is the principal inhibitor of tissue plasminogen activator (tPA) and urokinase (uPA), the activators of plasminogen and hence fibrinolysis (the physiological breakdown of blood clots). It is a serine protease inhibitor (serpin) protein (SERPINE1).

The other PAI, plasminogen activator inhibitor-2 (PAI-2) is secreted by the placenta and only present in significant amounts during pregnancy. In addition, protease nexin acts as an inhibitor of tPA and urokinase. PAI-1, however, is the main inhibitor of the plasminogen activators.

Genetics

The PLANH1 gene is located on the seventh chromosome (7q21.3-q22). There is a common polymorphism known as 4G/5G in the promoter region. The 5G allele is slightly less transcriptionally active than the 4G.

Function

PAI-1 is mainly produced by the endothelium (cells lining blood vessels), but is also secreted by other tissue types, such as adipose tissue.

PAI-1 inhibits the serine proteases tPA and uPA/urokinase, and hence is an inhibitor of fibrinolysis, the physiological process that degrades blood clots.

Fibrinolysis (simplified). Blue arrows denote stimulation, and red arrows inhibition.

Role in disease

Congenital deficiency of PAI-1 has been reported; as fibrinolysis is not suppressed adequately, it leads to a hemorrhagic diathesis (a tendency to hemorrhage).

PAI-1 is present in increased levels in various disease states (such as a number of forms of cancer), as well as in obesity and the metabolic syndrome. It has been linked to the increased occurrence of thrombosis in patients with these conditions.

In inflammatory conditions in which fibrin is deposited in tissues, PAI-1 appears to play a significant role in the progression to fibrosis (pathological formation of connective tissue). Presumably, lower PAI levels would lead to less suppression of fibrinolysis and conversely a more rapid degradation of the fibrin.

Angiotensin II inceases synthesis of plasminogen activator inhibitor-1, so it accelerates the development of atherosclerosis.

Pharmacology

Tiplaxtinin (PAI-039) is a small molecule inhibitor that is being studied for use in the attenuation of remodeling of blood vessels, a result of arterial hypertension and activation of the renin-angiotensin system.[1]

References

  1. Elokdah H, Abou-Gharbia M, Hennan JK, McFarlane G, Mugford CP, Krishnamurthy G, Crandall DL. Tiplaxtinin, a novel, orally efficacious inhibitor of plasminogen activator inhibitor-1: design, synthesis, and preclinical characterization. J Med Chem 2004;47:3491-4. PMID 15214776.

Further reading

  • Mimuro J (1991). "[Type 1 plasminogen activator inhibitor: its role in biological reactions]". Rinsho Ketsueki. 32 (5): 487–9. PMID 1870265. 
  • Binder BR, Christ G, Gruber F; et al. (2002). "Plasminogen activator inhibitor 1: physiological and pathophysiological roles.". News Physiol. Sci. 17: 56–61. PMID 11909993. 
  • Eddy AA (2002). "Plasminogen activator inhibitor-1 and the kidney.". Am. J. Physiol. Renal Physiol. 283 (2): F209–20. PMID 12110504. doi:10.1152/ajprenal.00032.2002. 
  • Schroeck F, Arroyo de Prada N, Sperl S; et al. (2003). "Interaction of plasminogen activator inhibitor type-1 (PAI-1) with vitronectin (Vn): mapping the binding sites on PAI-1 and Vn.". Biol. Chem. 383 (7-8): 1143–9. PMID 12437099. 
  • Gils A, Declerck PJ (2004). "The structural basis for the pathophysiological relevance of PAI-I in cardiovascular diseases and the development of potential PAI-I inhibitors.". Thromb. Haemost. 91 (3): 425–37. PMID 14983217. doi:10.1160/TH03-12-0764. 
  • Durand MK, Bødker JS, Christensen A; et al. (2004). "Plasminogen activator inhibitor-I and tumour growth, invasion, and metastasis.". Thromb. Haemost. 91 (3): 438–49. PMID 14983218. doi:10.1160/TH03-12-0784. 
  • Harbeck N, Kates RE, Gauger K; et al. (2004). "Urokinase-type plasminogen activator (uPA) and its inhibitor PAI-I: novel tumor-derived factors with a high prognostic and predictive impact in breast cancer.". Thromb. Haemost. 91 (3): 450–6. PMID 14983219. doi:10.1160/TH03-12-0798. 
  • Hertig A, Rondeau E (2004). "Plasminogen activator inhibitor type 1: the two faces of the same coin.". Curr. Opin. Nephrol. Hypertens. 13 (1): 39–44. PMID 15090858. 
  • Hoekstra T, Geleijnse JM, Schouten EG, Kluft C (2004). "Plasminogen activator inhibitor-type 1: its plasma determinants and relation with cardiovascular risk.". Thromb. Haemost. 91 (5): 861–72. PMID 15116245. doi:10.1267/THRO04050861. 
  • Lijnen HR (2005). "Pleiotropic functions of plasminogen activator inhibitor-1.". J. Thromb. Haemost. 3 (1): 35–45. PMID 15634264. doi:10.1111/j.1538-7836.2004.00827.x. 
  • De Taeye B, Smith LH, Vaughan DE (2005). "Plasminogen activator inhibitor-1: a common denominator in obesity, diabetes and cardiovascular disease.". Current opinion in pharmacology. 5 (2): 149–54. PMID 15780823. doi:10.1016/j.coph.2005.01.007. 
  • Dellas C, Loskutoff DJ (2005). "Historical analysis of PAI-1 from its discovery to its potential role in cell motility and disease.". Thromb. Haemost. 93 (4): 631–40. PMID 15841306. doi:10.1160/TH05-01-0033. 
  • Könsgen D, Mustea A, Lichtenegger W, Sehouli J (2005). "[Role of PAI-1 in gynaecological malignancies]". Zentralblatt für Gynäkologie. 127 (3): 125–31. PMID 15915389. doi:10.1055/s-2005-836407. 
  • Vaughan DE (2005). "PAI-1 and atherothrombosis.". J. Thromb. Haemost. 3 (8): 1879–83. PMID 16102055. doi:10.1111/j.1538-7836.2005.01420.x. 
  • Hermans PW, Hazelzet JA (2007). "Plasminogen activator inhibitor type 1 gene polymorphism and sepsis.". Clin. Infect. Dis. 41 Suppl 7: S453–8. PMID 16237647. doi:10.1086/431996. 
  • Alessi MC, Poggi M, Juhan-Vague I (2007). "Plasminogen activator inhibitor-1, adipose tissue and insulin resistance.". Curr. Opin. Lipidol. 18 (3): 240–5. PMID 17495595. doi:10.1097/MOL.0b013e32814e6d29. 
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